Fatal acute haemolysis and methaemoglobinaemia in a man with renal failure and Alkaptonuria – Is nitisinone the solution?-Reference-Cited by-同舟云学术

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Fatal acute haemolysis and methaemoglobinaemia in a man with renal failure and Alkaptonuria – Is nitisinone the solution?

Published:2020-06 Issue: Volume:23 Page:100588
ISSN:2214-4269
Container-title:Molecular Genetics and Metabolism Reports
language:en
Short-container-title:Molecular Genetics and Metabolism Reports

Author:

Davison A.S.,Luangrath E.,Selvi E.,Ranganath L.R.

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology

Reference40 articles.

1. An update on molecular genetics of Alkaptonuria (AKU);Zatkova;J. Inherit. Metab. Dis.,2011

2. The molecular basis of alkaptonuria;Fernández-Cañón;Nat. Genet.,1996

3. Alkaptonuria - many questions answered, further challenges beckon;Davison;Ann. Clin. Biochem.,2019

4. Analysis of the life span of alkaptonuric patients. [Slovak];Srsen;Cas. Lek. Cesk.,1985

5. Natural history of alkaptonuria;Phornphutkul;N. Engl. J. Med.,2002

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1. Painted in black: deciphering the cornerstones of a challenging case;Internal and Emergency Medicine;2024-07-02

2. Alkaptonuria;Nature Reviews Disease Primers;2024-03-07

3. Alkaptonuria – Past, present and future;Advances in Clinical Chemistry;2023

4. Improving the clinical accuracy and flexibility of the Alkaptonuria severity score index;JIMD Reports;2022-05-10

5. Influence of nitisinone and its metabolites on l-tyrosine metabolism in a model system;Chemosphere;2022-01

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